Canonical Allele Identifier: CA1685227017
Gene: PMS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5986975G= , CM000669.2:g.5986975G= GRCh38
NC_000007.13:g.6026606G= , CM000669.1:g.6026606G= GRCh37
NC_000007.12:g.5993132G= NCBI36
NG_008466.1:g.27132C= , LRG_161:g.27132C=

Transcript Alleles

HGVS Amino-acid change
ENST00000699814.2:c.*1186C= ENSP00000514615.2:n.*1186C=
ENST00000699840.2:c.1787C= ENSP00000514638.2:p.Thr596=
ENST00000699930.2:c.1682C= ENSP00000514695.2:p.Thr561=
ENST00000406569.8:c.1678+112C= ENSP00000514464.1:n.1678+112C=
ENST00000644110.2:c.*1384C= ENSP00000496392.2:n.*1384C=
ENST00000699752.1:c.1634C= ENSP00000514561.1:p.Thr545=
ENST00000699753.1:c.*1211C= ENSP00000514562.1:n.*1211C=
ENST00000699754.1:c.1592C= ENSP00000514563.1:p.Thr531=
ENST00000699755.1:c.*1189C= ENSP00000514564.1:n.*1189C=
ENST00000699756.1:c.*1377C= ENSP00000514565.1:n.*1377C=
ENST00000699757.1:c.*1047C= ENSP00000514566.1:n.*1047C=
ENST00000699758.1:c.*1047C= ENSP00000514567.1:n.*1047C=
ENST00000699759.1:n.2644C=
ENST00000699760.1:c.1472C= ENSP00000514568.1:p.Thr491=
ENST00000699761.1:c.1385C= ENSP00000514569.1:p.Thr462=
ENST00000699762.1:c.1217C= ENSP00000514570.1:p.Thr406=
ENST00000699763.1:c.*880C= ENSP00000514571.1:n.*880C=
ENST00000699764.1:c.*108C= ENSP00000514572.1:n.*108C=
ENST00000699765.1:c.*886C= ENSP00000514573.1:n.*886C=
ENST00000699766.1:c.1790C= ENSP00000514574.1:p.Thr597=
ENST00000699767.1:c.1790C= ENSP00000514575.1:p.Thr597=
ENST00000699768.1:c.1790C= ENSP00000514576.1:p.Thr597=
ENST00000699811.1:c.1385C= ENSP00000514614.1:p.Thr462=
ENST00000699813.1:n.1903C=
ENST00000699814.1:c.1413C=
ENST00000699815.1:c.*1321C= ENSP00000514616.1:n.*1321C=
ENST00000699816.1:c.*680C= ENSP00000514617.1:n.*680C=
ENST00000699817.1:c.*1384C= ENSP00000514618.1:n.*1384C=
ENST00000699818.1:c.1385C= ENSP00000514619.1:p.Thr462=
ENST00000699819.1:c.*947C= ENSP00000514620.1:n.*947C=
ENST00000699820.1:c.1144+2825C= ENSP00000514621.1:n.1144+2825C=
ENST00000699821.1:c.1385C= ENSP00000514622.1:p.Thr462=
ENST00000699822.1:c.*1242C= ENSP00000514623.1:n.*1242C=
ENST00000699823.1:c.1385C= ENSP00000514624.1:p.Thr462=
ENST00000699824.1:c.*1293C= ENSP00000514625.1:n.*1293C=
ENST00000699825.1:c.1229C= ENSP00000514626.1:p.Thr410=
ENST00000699826.1:c.*1189C= ENSP00000514627.1:n.*1189C=
ENST00000699827.1:c.1622C= ENSP00000514628.1:p.Thr541=
ENST00000699828.1:c.*880C= ENSP00000514629.1:n.*880C=
ENST00000699833.1:n.3562C=
ENST00000699837.1:c.1385C= ENSP00000514635.1:p.Thr462=
ENST00000699838.1:c.*1690C= ENSP00000514636.1:n.*1690C=
ENST00000699839.1:c.1976C= ENSP00000514637.1:p.Thr659=
ENST00000699916.1:c.*1047C= ENSP00000514684.1:n.*1047C=
ENST00000699917.1:c.*1239C= ENSP00000514685.1:n.*1239C=
ENST00000699918.1:c.*1291C= ENSP00000514686.1:n.*1291C=
ENST00000699919.1:c.*1377C= ENSP00000514687.1:n.*1377C=
ENST00000699920.1:c.*1426C= ENSP00000514688.1:n.*1426C=
ENST00000699928.1:c.989-3984C= ENSP00000514693.1:n.989-3984C=
ENST00000699929.1:c.*1091C= ENSP00000514694.1:n.*1091C=
ENST00000699930.1:c.1682C= ENSP00000514695.1:p.Thr561=
ENST00000699931.1:n.3218C=
ENST00000699951.1:c.*886C= ENSP00000514706.1:n.*886C=
ENST00000699952.1:c.803+10351C= ENSP00000514707.1:n.803+10351C=
ENST00000699953.1:c.*897C= ENSP00000514708.1:n.*897C=
ENST00000699954.1:c.*1091C= ENSP00000514709.1:n.*1091C=
ENST00000265849.12:c.1790C= MANE Select ENSP00000265849.7:p.Thr597=
ENST00000642292.1:c.1385C= ENSP00000495524.1:p.Thr462=
ENST00000642456.1:c.1385C= ENSP00000493814.1:p.Thr462=
ENST00000643595.1:c.*1189C= ENSP00000494497.1:n.*1189C=
ENST00000644110.1:c.1472C= ENSP00000496392.1:p.Thr491=
ENST00000265849.11:c.1790C= ENSP00000265849.7:p.Thr597=
ENST00000382321.5:c.804-3984C= ENSP00000371758.4:n.804-3984C=
ENST00000406569.7:n.1678+112C=
ENST00000441476.6:c.1472C= ENSP00000392843.2:p.Thr491=
ENST00000469652.1:n.63-4070C=
NM_000535.5:c.1790C= , LRG_161t1:c.1790C= NP_000526.1:p.Thr597=
NR_003085.2:n.1872C=
XM_006715742.2:c.1784C= XP_006715805.1:p.Thr595=
XM_006715744.2:c.857C= XP_006715807.1:p.Thr286=
XM_011515427.1:c.1835C= XP_011513729.1:p.Thr612=
XM_011515428.1:c.1679C= XP_011513730.1:p.Thr560=
XM_011515429.1:c.1472C= XP_011513731.1:p.Thr491=
XM_011515430.1:c.1472C= XP_011513732.1:p.Thr491=
NM_000535.6:c.1790C= NP_000526.2:p.Thr597=
NM_001322003.1:c.1385C= NP_001308932.1:p.Thr462=
NM_001322004.1:c.1385C= NP_001308933.1:p.Thr462=
NM_001322005.1:c.1385C= NP_001308934.1:p.Thr462=
NM_001322006.1:c.1634C= NP_001308935.1:p.Thr545=
NM_001322007.1:c.1472C= NP_001308936.1:p.Thr491=
NM_001322008.1:c.1472C= NP_001308937.1:p.Thr491=
NM_001322009.1:c.1385C= NP_001308938.1:p.Thr462=
NM_001322010.1:c.1229C= NP_001308939.1:p.Thr410=
NM_001322011.1:c.857C= NP_001308940.1:p.Thr286=
NM_001322012.1:c.857C= NP_001308941.1:p.Thr286=
NM_001322013.1:c.1217C= NP_001308942.1:p.Thr406=
NM_001322014.1:c.1790C= NP_001308943.1:p.Thr597=
NM_001322015.1:c.1481C= NP_001308944.1:p.Thr494=
NR_136154.1:n.1877C=
XM_006715744.4:c.857C= XP_006715807.1:p.Thr286=
XM_017012342.2:c.857C= XP_016867831.1:p.Thr286=
XM_024446800.1:c.1229C= XP_024302568.1:p.Thr410=
NM_000535.7:c.1790C= MANE Select NP_000526.2:p.Thr597=
NM_001322003.2:c.1385C= NP_001308932.1:p.Thr462=
NM_001322004.2:c.1385C= NP_001308933.1:p.Thr462=
NM_001322005.2:c.1385C= NP_001308934.1:p.Thr462=
NM_001322006.2:c.1634C= NP_001308935.1:p.Thr545=
NM_001322008.2:c.1472C= NP_001308937.1:p.Thr491=
NM_001322009.2:c.1385C= NP_001308938.1:p.Thr462=
NM_001322010.2:c.1229C= NP_001308939.1:p.Thr410=
NM_001322011.2:c.857C= NP_001308940.1:p.Thr286=
NM_001322012.2:c.857C= NP_001308941.1:p.Thr286=
NM_001322013.2:c.1217C= NP_001308942.1:p.Thr406=
NM_001322014.2:c.1790C= NP_001308943.1:p.Thr597=
NM_001322015.2:c.1481C= NP_001308944.1:p.Thr494=
NM_001322007.2:c.1472C= NP_001308936.1:p.Thr491=